nuclear RNA export factor 5, isoform CRA_b [Homo sapiens]

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Inv(X)(p21.1;q22.1) in a man with mental retardation, short stature, general muscle wasting, and facial dysmorphism: clinical study and mutation analysis of the NXF5 gene. [Am J Med Genet A. 2003]
Inv(X)(p21.1;q22.1) in a man with mental retardation, short stature, general muscle wasting, and facial dysmorphism: clinical study and mutation analysis of the NXF5 gene.
Frints SG, Jun L, Fryns JP, Devriendt K, Teulingkx R, Van den Berghe L, De Vos B, Borghgraef M, Chelly J, Des Portes V, et al. Am J Med Genet A. 2003 Jun 15; 119A(3):367-74.
Unique X-linked familial FSGS with co-segregating heart block disorder is associated with a mutation in the NXF5 gene. [Hum Mol Genet. 2013]
Unique X-linked familial FSGS with co-segregating heart block disorder is associated with a mutation in the NXF5 gene.
Esposito T, Lea RA, Maher BH, Moses D, Cox HC, Magliocca S, Angius A, Nyholt DR, Titus T, Kay T, et al. Hum Mol Genet. 2013 Sep 15; 22(18):3654-66. Epub 2013 May 16.
Formation of a Tap/NXF1 homotypic complex is mediated through the amino-terminal domain of Tap and enhances interaction with nucleoporins. [Mol Biol Cell. 2008]
Formation of a Tap/NXF1 homotypic complex is mediated through the amino-terminal domain of Tap and enhances interaction with nucleoporins.
Matzat LH, Berberoglu S, Lévesque L. Mol Biol Cell. 2008 Jan; 19(1):327-38. Epub 2007 Oct 31.

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